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132933-15-4

ethyl 2-[(5-methyl-2-oxo-1,2,4,5-tetrahydroimidazo[4,5,1-jk][1,4]benzodiazepin-6(7H)-yl)methyl]prop-2-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132933-15-4 Structure

  • Basic information

    1. Product Name: ethyl 2-[(5-methyl-2-oxo-1,2,4,5-tetrahydroimidazo[4,5,1-jk][1,4]benzodiazepin-6(7H)-yl)methyl]prop-2-enoate
    2. Synonyms: 6-(2-Ethoxycarbonyl-propen-3-yl)-4,5,6,7-tetrahydro-5-methylimidazo(4,5,1-jk)(1,4)benzodiazepin-2(1H)-one; 6-(2-Ethoxycarbonyl-propen-3-yl)-4,5,6,7-tetrahydro-5-methylimidazo[4,5,1-jk][1,4]benzodiazepin-2(1H)-one; ethyl 2-[(2-hydroxy-5-methyl-4,5-dihydroimidazo[4,5,1-jk][1,4]benzodiazepin-6(7H)-yl)methyl]prop-2-enoate; Imidazo(4,5,1-jk)(1,4)benzodiazepine-6(7H)-propanoic acid, 1,2,4,5-tetrahydro-5-methyl-alpha-methylene-2-oxo-, ethyl ester; Imidazo[4,5,1-jk][1,4]benzodiazepine-6(7H)-propanoic acid, 1,2,4,5-tetrahydro-5-methyl-.alpha.-methylene-2-oxo-, ethyl ester; imidazo[4,5,1-jk][1,4]benzodiazepine-6(7H)-propanoic acid, 4,5-dihydro-2-hydroxy-5-methyl-alpha-methylene-, ethyl ester
    3. CAS NO:132933-15-4
    4. Molecular Formula: C17H21N3O3
    5. Molecular Weight: 315.3669
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132933-15-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: 1.27g/cm3
    6. Refractive Index: 1.613
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: ethyl 2-[(5-methyl-2-oxo-1,2,4,5-tetrahydroimidazo[4,5,1-jk][1,4]benzodiazepin-6(7H)-yl)methyl]prop-2-enoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-[(5-methyl-2-oxo-1,2,4,5-tetrahydroimidazo[4,5,1-jk][1,4]benzodiazepin-6(7H)-yl)methyl]prop-2-enoate(132933-15-4)
    11. EPA Substance Registry System: ethyl 2-[(5-methyl-2-oxo-1,2,4,5-tetrahydroimidazo[4,5,1-jk][1,4]benzodiazepin-6(7H)-yl)methyl]prop-2-enoate(132933-15-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 132933-15-4(Hazardous Substances Data)

132933-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132933-15-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,9,3 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 132933-15:
(8*1)+(7*3)+(6*2)+(5*9)+(4*3)+(3*3)+(2*1)+(1*5)=114
114 % 10 = 4
So 132933-15-4 is a valid CAS Registry Number.

132933-15-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 132933-15-4

1.2 Other means of identification

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Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

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More Details:132933-15-4 SDS

132933-15-4Downstream Products

132933-15-4Relevant articles and documents

Synthesis and Anti-HIV-1 Activity of 4,5,6,7-Tetrahydro-5-methylimidazobenzodiazepin-2(1H)-one (TIBO) Derivatives

Kukla, Michael J.,Breslin, Henry J.,Pauwels, Rudi,Fedde, Cynthia L.,Miranda, Milton,et al.

, p. 746 - 751 (2007/10/02)

A series of 6-substituted 4,5,6,7-tetrahydro-5-methylimidazobenzodiazepin-2(1H)-ones (9) have been synthesized and tested for their ability to inhibit the replication of the HIV-1 virus in MT-4 cells.Two synthetic methods are described, one of which allows the synthesis of single enantiomers of the final products.A structure-activity study was done within the series of compounds to determine the optimum group for the 6-position substitution and to determine whether the activity was enantiospecific at the 5-position, which was substituted with a methyl group.The best analogue, 9jj, inhibited HIV-1 with an IC50 of 4 μM, which is comparable to the activity level of DDI, a 2',3'-dideoxynucleoside-type structure undergoing clinical trials as an anti-AIDS therapy.

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